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Altered microRNA profiles in plasma exosomes from mesial temporal lobe epilepsy with hippocampal sclerosis
Mesial temporal lobe epilepsy with hippocampal sclerosis (mTLE-HS) is the most common type of focal epilepsy. The present study aimed to explore the expression and functions of exosomal microRNAs in mTLE-HS. A total of 50 microRNAs were found to be differentially expressed in mTLE-HS compared with h...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5354818/ https://www.ncbi.nlm.nih.gov/pubmed/27926529 http://dx.doi.org/10.18632/oncotarget.13744 |
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author | Yan, Shaofeng Zhang, Hua Xie, Wenyan Meng, Fangang Zhang, Kai Jiang, Yin Zhang, Xin Zhang, Jianguo |
author_facet | Yan, Shaofeng Zhang, Hua Xie, Wenyan Meng, Fangang Zhang, Kai Jiang, Yin Zhang, Xin Zhang, Jianguo |
author_sort | Yan, Shaofeng |
collection | PubMed |
description | Mesial temporal lobe epilepsy with hippocampal sclerosis (mTLE-HS) is the most common type of focal epilepsy. The present study aimed to explore the expression and functions of exosomal microRNAs in mTLE-HS. A total of 50 microRNAs were found to be differentially expressed in mTLE-HS compared with healthy controls. Among them, 2 were increased and 48 were decreased. The 6 significant differentially expressed candidate microRNAs (miR-3613-5p, miR-4668-5p, miR-8071, miR-197-5p, miR-4322, and miR-6781-5p ) in exosome were validated. The bioinformatics analysis showed that the potential target genes of these microRNAs were involved in biological processes, molecular functions, and cellular components. Similarly, these microRNAs also affected axon guidance, pathways in cancer, regulation of the actin cytoskeleton, focal adhesion, the calcium signaling pathway, the MAPK signaling pathway, and the PI3K-Akt signaling pathway. Among 6 candidate microRNAs, miR-8071 had the best diagnostic value for mTLE-HS with 83.33% sensitivity and 96.67% specificity, and was associated with seizure severity. This study indicated that exosomal microRNAs, may be regulators for the seizure development in mTLE-HS, and can be used as potential therapeutic targets and biomarker for diagnosis in mTLE-HS. |
format | Online Article Text |
id | pubmed-5354818 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-53548182017-04-24 Altered microRNA profiles in plasma exosomes from mesial temporal lobe epilepsy with hippocampal sclerosis Yan, Shaofeng Zhang, Hua Xie, Wenyan Meng, Fangang Zhang, Kai Jiang, Yin Zhang, Xin Zhang, Jianguo Oncotarget Research Paper Mesial temporal lobe epilepsy with hippocampal sclerosis (mTLE-HS) is the most common type of focal epilepsy. The present study aimed to explore the expression and functions of exosomal microRNAs in mTLE-HS. A total of 50 microRNAs were found to be differentially expressed in mTLE-HS compared with healthy controls. Among them, 2 were increased and 48 were decreased. The 6 significant differentially expressed candidate microRNAs (miR-3613-5p, miR-4668-5p, miR-8071, miR-197-5p, miR-4322, and miR-6781-5p ) in exosome were validated. The bioinformatics analysis showed that the potential target genes of these microRNAs were involved in biological processes, molecular functions, and cellular components. Similarly, these microRNAs also affected axon guidance, pathways in cancer, regulation of the actin cytoskeleton, focal adhesion, the calcium signaling pathway, the MAPK signaling pathway, and the PI3K-Akt signaling pathway. Among 6 candidate microRNAs, miR-8071 had the best diagnostic value for mTLE-HS with 83.33% sensitivity and 96.67% specificity, and was associated with seizure severity. This study indicated that exosomal microRNAs, may be regulators for the seizure development in mTLE-HS, and can be used as potential therapeutic targets and biomarker for diagnosis in mTLE-HS. Impact Journals LLC 2016-12-01 /pmc/articles/PMC5354818/ /pubmed/27926529 http://dx.doi.org/10.18632/oncotarget.13744 Text en Copyright: © 2017 Yan et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Yan, Shaofeng Zhang, Hua Xie, Wenyan Meng, Fangang Zhang, Kai Jiang, Yin Zhang, Xin Zhang, Jianguo Altered microRNA profiles in plasma exosomes from mesial temporal lobe epilepsy with hippocampal sclerosis |
title | Altered microRNA profiles in plasma exosomes from mesial temporal lobe epilepsy with hippocampal sclerosis |
title_full | Altered microRNA profiles in plasma exosomes from mesial temporal lobe epilepsy with hippocampal sclerosis |
title_fullStr | Altered microRNA profiles in plasma exosomes from mesial temporal lobe epilepsy with hippocampal sclerosis |
title_full_unstemmed | Altered microRNA profiles in plasma exosomes from mesial temporal lobe epilepsy with hippocampal sclerosis |
title_short | Altered microRNA profiles in plasma exosomes from mesial temporal lobe epilepsy with hippocampal sclerosis |
title_sort | altered microrna profiles in plasma exosomes from mesial temporal lobe epilepsy with hippocampal sclerosis |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5354818/ https://www.ncbi.nlm.nih.gov/pubmed/27926529 http://dx.doi.org/10.18632/oncotarget.13744 |
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